Canonical Allele Identifier: CA361759963

Gene: CSF1R

Linked Data

• gnomAD v4: 5-150057306-G-A
• MyVariant Identifiers: chr5:g.149436869G>A (hg19) ; chr5:g.150057306G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.150057306G>A , CM000667.2:g.150057306G>A	GRCh38
NC_000005.9:g.149436869G>A , CM000667.1:g.149436869G>A	GRCh37
NC_000005.8:g.149417062G>A	NCBI36
NG_012303.1:g.61067C>T
NG_012303.2:g.61067C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675795.1:c.2300C>T MANE Select	ENSP00000501699.1:p.Ala767Val
ENST00000286301.7:c.2300C>T	ENSP00000286301.3:p.Ala767Val
ENST00000504875.5:c.*121C>T	ENSP00000422212.1:n.*121C>T
ENST00000515068.1:c.469C>T	ENSP00000427545.1:n.469C>T
NM_001288705.1:c.2300C>T	NP_001275634.1:p.Ala767Val
NM_005211.3:c.2300C>T	NP_005202.2:p.Ala767Val
NR_109969.1:n.2350C>T
NM_001288705.2:c.2300C>T	NP_001275634.1:p.Ala767Val
NM_001349736.1:c.2300C>T	NP_001336665.1:p.Ala767Val
NM_001288705.3:c.2300C>T MANE Select	NP_001275634.1:p.Ala767Val
NM_001375320.1:c.2300C>T	NP_001362249.1:p.Ala767Val
NM_001375321.1:c.1856C>T	NP_001362250.1:p.Ala619Val
NR_164679.1:n.2193C>T
NM_001349736.2:c.2300C>T	NP_001336665.1:p.Ala767Val
NM_005211.4:c.2300C>T	NP_005202.2:p.Ala767Val
NR_109969.2:n.2264C>T